Beschreibung
About Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
We have a new and exciting opportunity to hire a Medical Safety Specialist for our Pharmacovigilance (Local Medical Safety) team at Hong Kong office!
Job Purpose and Scope:
Supporting that the LOC Safety activities, related to medicinal and non-medicinal products are managed in compliance with local regulations and company policies/procedures at a local, regional and global levels and in accordance with any Product vigilance agreements with third party business partners.
Having appropriate Pharmacovigilance and Risk Management systems in place to assure appropriate oversight for products within its responsibility.
Key Responsibilities:
- Support that systems and processes are available for collection and reporting of safety information to meet local and global requirements
- Maintain oversight on day-to-day AE inbound and outbound reporting as applicable
- Oversee data generating activities to ensure appropriate review and reporting process are included in project documents for reporting potential AEs (e.g. patient support programs, market research surveys, internet sites)
- Ensure that day-to-day PV functions are performed satisfactorily, and that optimal regulatory compliance is maintained at the LOC level.
- Maintain overall responsibility for the coordination of safety requirements as delegated by Marketing Authorization Holders (MAH).
- Coordinate and support local PV audit and inspection.
- Ensure awareness of changes in regulations which may have an impact on vigilance activities and responsibilities. Evaluate the impact on local processes and inform the appropriate global and regional groups
- Ensure adequate local signal detection process if required and ensure reporting of potential single case signals or clusters of similar events seen in case processing
- Build and maintain effective business relationships across the LOC.
Risk Management:
- Have an appropriate system of Risk Management in place in order to assure appropriate oversight for products
- Review and complete country specific Annex as required according to local requirements, if applicable
- Collaborate with Medical Affairs and Regulatory Affairs team to ensure that RMP activities are completed on a timely manner
- Ensure implementation and tracking of RMP activities are in place including documentation of completed activities
- Review all risk management plans and PSURs to obtain information on the risk/benefit profile of products
- Provide MS input in pre-authorisation phase/submission-planning phase of product lifecycle to guide appropriate planning and management of RMP-related activities.
Befähigungen
Qualifications
Education:
- Medical, pharmacy or health sciences background with confirmed expertise and experience in pharmaceutical regulation
Experience and Skills:
Required:
- 2+ years of experience in PV/Medical safety related field essential; experience working in the pharmaceutical industry is strongly preferred
- Experience in audit and conducting training
- Demonstrated attention to detail
- Effective decision maker to assess impact of actions taken locally on the global PV system
- High customer orientation
- Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
- Sound judgment, strong planning and organizational skills, and the ability to get things done
- Demonstrated strong sense of urgency
- Strong influencing skills to explain and defend a position which is in the best interests of patient safety
Other:
- Fluency in written and oral English and Cantonese to facilitate communications with GMO, regional Medical, other global functions, and Health Authority
This Is What Awaits YOU At J&J
- An opportunity to be part of a global market leader.
- A dynamic and inspiring working environment.
- Many opportunities to work on challenging pro jects and assignments.
- Possibilities for further personal as well as professional development.
- Many employees benefits:
- Supportive team culture, flexible working hours, employee development and wellness support,
- Refreshment in the workplace, company gym, JJ Club, corporate events
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.